Infusion Set
Ref 2002,2003,IV-2010,IV-2009,IV-2009/1,750026,750036,750046,750076,750096,750106,750016,750035,750038 and 750040Model 2002, 2003, IV-2010, IV-2009, IV-2009/1, 2002+N, 200059-125, 200059,,2003+N,200059-175,200059-230, 750026, 750036, 750046, 750076, 750096, 750106, 750016, 750035, 750038 and 750040
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-InfusionLZ D-InfusionLZ | Date20 Sep 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / Reference
- 2002, 2003, IV-2010, IV-2009, IV-2009/1, 2002+N, 200059-125, 200059, 2003+N, 200059-175, 200059-230, 750026, 750036, 750046, 750076, 750096, 750106, 750016, 750035, 750038 and 750040
- Primary DI / UDI-DI
- D-InfusionLZ
- Basic UDI-DI
- B-InfusionLZ
- EMDN Code
- A03040199 Infusion kits (with or w/o pump), single-use - other
- Device Class
- Class IIa
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- EG-MF-000025747
- Authorised representative
- Allmed Medical GmbH DE-AR-000007830
Other devices from Allmed Middle East
Properties
Other properties (10)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No